A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3565081



Internal ID22433803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21900387..21900387hg38UCSC Ensembl
chr7:21940005..21940005hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14333020
SamplesHG00731
Known GenesDNAH11
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3565081
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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